The Burden of Multiple Myeloma on Patients and Caregivers Quality of Life: a Canadian Real-World Study
1 other identifier
observational
400
1 country
1
Brief Summary
The purpose of this observational study is to estimate the burden of multiple myeloma on patients and caregivers in terms of QoL. Additionally, this study will assess the correlation between QoL, obtained from commonly used and validated questionnaires, and the perceptions of both patients and caregivers respectively., obtain from a 10-point scale and a comment box.
Trial Health
Trial Health Score
Automated assessment based on enrollment pace, timeline, and geographic reach
participants targeted
Target at P75+ for all trials
Started Oct 2024
Shorter than P25 for all trials
1 active site
Health score is calculated from publicly available data and should be used for screening purposes only.
Trial Relationships
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Study Timeline
Key milestones and dates
First Submitted
Initial submission to the registry
September 12, 2024
CompletedFirst Posted
Study publicly available on registry
September 24, 2024
CompletedStudy Start
First participant enrolled
October 15, 2024
CompletedPrimary Completion
Last participant's last visit for primary outcome
February 24, 2025
CompletedStudy Completion
Last participant's last visit for all outcomes
March 12, 2025
CompletedMarch 13, 2025
March 1, 2025
4 months
September 12, 2024
March 12, 2025
Conditions
Keywords
Outcome Measures
Primary Outcomes (1)
To estimate quality of life of patients with myeloma and caregivers of patients with myeloma
From enrollment until sample size is reached
Secondary Outcomes (1)
To assess the correlation between QoL scores and perception of patients and caregivers respectively
From recruitment until sample size is reached
Study Arms (2)
Patients with multiple myeloma
Patients with multiple myeloma member of Myeloma Canada database
Caregivers of patients with myeloma
Caregiver of a multiple myeloma patient member of Myeloma Canada database
Interventions
No specific intervention is assess in this study.
Eligibility Criteria
Patients with myeloma and caregivers of patients with myeloma who are part of Myeloma Canada database
You may qualify if:
- years of age or older;
- Part of the Myeloma Canada database;
- Identified as a patient with MM or
- Identified as a current caregiver of a patient with MM at the time of participation.
- Ability to read and understand English or French;
- Signature of informed consent form (ICF).
Contact the study team to confirm eligibility.
Sponsors & Collaborators
- PeriPharmlead
Study Sites (1)
PROxy Network, an initiative of PeriPharm inc.
Montreal, Quebec, H2Y 2H4, Canada
MeSH Terms
Conditions
Condition Hierarchy (Ancestors)
Study Design
- Study Type
- observational
- Observational Model
- COHORT
- Time Perspective
- CROSS SECTIONAL
- Sponsor Type
- OTHER
- Responsible Party
- SPONSOR
Study Record Dates
First Submitted
September 12, 2024
First Posted
September 24, 2024
Study Start
October 15, 2024
Primary Completion
February 24, 2025
Study Completion
March 12, 2025
Last Updated
March 13, 2025
Record last verified: 2025-03
Data Sharing
- IPD Sharing
- Will not share